首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Quality evaluation of Guan‐Xin‐Ning injection based on fingerprint analysis and simultaneous separation and determination of seven bioactive constituents by capillary electrophoresis
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Quality evaluation of Guan‐Xin‐Ning injection based on fingerprint analysis and simultaneous separation and determination of seven bioactive constituents by capillary electrophoresis

机译:基于指纹分析的关 - 新宁注射液及毛细管电泳同时分离和测定七种生物活性成分的质量评价

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摘要

Abstract The purpose of this study was to develop a comprehensive, rapid and practical capillary electrophoresis (CE) method for quality control (QC) of Guan‐Xin‐Ning (GXN) injection based on fingerprint analysis and simultaneous separation and determination of seven constituents. In fingerprint analysis, a capillary zone electrophoresis (CZE) method with a running buffer of 30 mM borate solution (pH 9.3) was established. Meanwhile, ten batches of samples were used to establish the fingerprint electropherogram and 34 common peaks were obtained within 20 min. The RSD of relative migration times (RMT) and relative peak areas (RPA) were less than 5%. In order to further evaluate the quality of GXN injection, a micellar electrokinetic chromatography (MEKC) method was developed for simultaneous separation and determination of bioactive constituents. Seven components reached baseline separation with a running buffer containing 35 mM SDS and 45 mM borate solution (pH 9.3). A good linearity was obtained with correlation coefficients from 0.9906 to 0.9997. The LOD and LOQ ranged from 0.12 to 1.50 μg/mL and from 0.40 to 4.90 μg/mL, respectively. The recoveries ranged between 99.0 and 104.4%. Therefore, it was concluded that the proposed method can be used for full‐scale quality analysis of GXN injection.
机译:摘要本研究的目的是,基于指纹分析和同时分离和测定七种成分的杂志注射液的全面,快速和实用的毛细管电泳(CE)方法,用于围Xin-ning(GXN)注射液的质量控制(QC)。在指纹分析中,建立了具有30mM硼酸盐溶液(pH9.3)的运行缓冲液的毛细管区电泳(CZE)方法。同时,10批样品用于建立指纹电泳图,在20分钟内获得34个常见峰。相对迁移时间(RMT)和相对峰面积(RPA)的RSD小于5%。为了进一步评估GXN注射的质量,开发了一种胶束电动色谱(MEKC)方法以同时分离和测定生物活性成分。七种组分达到基线分离,其运行缓冲液含有35mM SDS和45mM硼酸盐溶液(pH9.3)。使用0.9906至0.9997的相关系数获得良好的线性度。 LOD和LOQ分别为0.12至1.50μg/ ml,分别为0.40至4.90μg/ ml。回收率范围为99.0至104.4%。因此,得出结论,该方法可用于GXN注射的全规模质量分析。

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